@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP940384.RAwxwWoH7g-OoLY2SmcsJk_O8jXquMQgp1yeFuulgpu-I> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP940384.RAwxwWoH7g-OoLY2SmcsJk_O8jXquMQgp1yeFuulgpu-I130_head {
  this: np:hasAssertion dgn-np:NP940384.RAwxwWoH7g-OoLY2SmcsJk_O8jXquMQgp1yeFuulgpu-I130_assertion ;
    np:hasProvenance dgn-np:NP940384.RAwxwWoH7g-OoLY2SmcsJk_O8jXquMQgp1yeFuulgpu-I130_provenance ;
    np:hasPublicationInfo dgn-np:NP940384.RAwxwWoH7g-OoLY2SmcsJk_O8jXquMQgp1yeFuulgpu-I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP940384.RAwxwWoH7g-OoLY2SmcsJk_O8jXquMQgp1yeFuulgpu-I130_assertion a np:Assertion .
  dgn-np:NP940384.RAwxwWoH7g-OoLY2SmcsJk_O8jXquMQgp1yeFuulgpu-I130_provenance a np:Provenance .
  dgn-np:NP940384.RAwxwWoH7g-OoLY2SmcsJk_O8jXquMQgp1yeFuulgpu-I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP940384.RAwxwWoH7g-OoLY2SmcsJk_O8jXquMQgp1yeFuulgpu-I130_assertion {
  miriam-gene:2261 a ncit:C16612 .
  lld:C0029434 a ncit:C7057 .
  dgn-gda:DGNe519c19b987370fb8c181c3dd19ea9a0 sio:SIO_000628 miriam-gene:2261 , lld:C0029434 ;
    a sio:SIO_001121 .
}
dgn-np:NP940384.RAwxwWoH7g-OoLY2SmcsJk_O8jXquMQgp1yeFuulgpu-I130_provenance {
  dgn-np:NP940384.RAwxwWoH7g-OoLY2SmcsJk_O8jXquMQgp1yeFuulgpu-I130_assertion dcterms:description "[The number of birth defect cases in the Texas Birth Defects Registry (one of the largest active birth defects surveillance systems in the world) enabled us to examine six different heritable disorders (aqueductal stenosis, infantile polycystic kidney disease, achondroplasia, thanatophoric dwarfism, chondrodysplasia/dwarfism not otherwise specified (NOS), and osteogenesis imperfecta) for a variety of descriptive demographic variables.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:22102535 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP940384.RAwxwWoH7g-OoLY2SmcsJk_O8jXquMQgp1yeFuulgpu-I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:51+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetv3.0rdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v4.0.0.0" .
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}